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(PAC) Rev 24 Based on Applicable Aegls, Erpgs, Or Teels (Chemicals Listed by CASRN) PAC Rev 24 – August 2008
Table 3: Protective Action Criteria (PAC) Rev 24 based on applicable AEGLs, ERPGs, or TEELs (Chemicals listed By CASRN) PAC Rev 24 – August 2008 Table 3 presents a listing of chemicals and PAC data based on the Chemical Abstract Service Registry Numbers (CASRNs)1 of the chemicals. Chemicals without an identified CASRN number are issued an identification number, preceded by the letter “z,” for purposes of the PAC data set. The columns presented in Table 3 provide the following information: Heading Definition No. The ordered numbering of the chemicals as they appear in this listing by CASRN. Chemical Name The common name of the chemical. CASRN The Chemical Abstract Service Registry Number for this chemical. TEEL-0 This is the threshold concentration below which most people will experience no appreciable risk of health effects. This PAC is always based on TEEL-0 because AEGL-0 or ERPG-0 values do not exist. PAC-1 Based on the applicable AEGL-1, ERPG-1, or TEEL-1 value. PAC-2 Based on the applicable AEGL-2, ERPG-2, or TEEL-2 value. PAC-3 Based on the applicable AEGL-3, ERPG-3, or TEEL-3 value. Units The units for the PAC values (ppm or mg/m3). Additional information on the chemicals presented here is provided in PAC Tables 1, 2, and 4. Table 3, other PAC Tables, introductory/explanatory material (including a glossary of acronyms and abbreviations), definitions of PAC values, and alternative methods of displaying PAC information are available electronically at: http://www.hss.energy.gov/HealthSafety/WSHP/chem_safety/teel.html. -
The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy”
chemengineering Article Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy” Robert J. Meier Pro-Deo Consultant, 52525 Heinsberg, North-Rhine Westphalia, Germany; [email protected] Abstract: Group contribution (GC) methods to predict thermochemical properties are of eminent importance to process design. Compared to previous works, we present an improved group contri- bution parametrization for the heat of formation of organic molecules exhibiting chemical accuracy, i.e., a maximum 1 kcal/mol (4.2 kJ/mol) difference between the experiment and model, while, at the same time, minimizing the number of parameters. The latter is extremely important as too many parameters lead to overfitting and, therewith, to more or less serious incorrect predictions for molecules that were not within the data set used for parametrization. Moreover, it was found to be important to explicitly account for common chemical knowledge, e.g., geminal effects or ring strain. The group-related parameters were determined step-wise: first, alkanes only, and then only one additional group in the next class of molecules. This ensures unique and optimal parameter values for each chemical group. All data will be made available, enabling other researchers to extend the set to other classes of molecules. Keywords: enthalpy of formation; thermodynamics; molecular modeling; group contribution method; quantum mechanical method; chemical accuracy; process design Citation: Meier, R.J. Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy”. 1. Introduction ChemEngineering 2021, 5, 24. To understand chemical reactivity and/or chemical equilibria, knowledge of thermo- o https://doi.org/10.3390/ dynamic properties such as gas-phase standard enthalpy of formation DfH gas is a necessity. -
Supporting Information
Photocatalytic Atom Transfer Radical Addition to Olefins utilizing Novel Photocatalysts Errika Voutyritsa, Ierasia Triandafillidi, Nikolaos V. Tzouras, Nikolaos F. Nikitas, Eleftherios K. Pefkianakis, Georgios C. Vougioukalakis* and Christoforos G. Kokotos* Laboratory of Organic Chemistry, Department of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis, Athens 15771, Greece SUPPORTING INFORMATION Page General Remarks S2 Optimization of the Reaction Conditions for the Photocatalytic Reaction S3 between 1-decene and BrCH2CN Synthesis of Photocatalysts S5 Synthesis of the Starting Materials S12 General Procedure for the Photocatalytic Reaction between Olefins and S18 BrCH2CN General Procedure for the Photocatalytic Reaction between Olefins and S29 BrCCl3 Determination of the Quantum Yield S33 Phosphorescence Quenching Studies S36 References S41 NMR Spectra S43 E. Voutyritsa, I. Triandafillidi, N. V. Tzouras, N. F. Nikitas, E. K. Pefkianakis, G. C. Vougioukalakis & C. G. Kokotos S1 General Remarks Chromatographic purification of products was accomplished using forced-flow ® chromatography on Merck Kieselgel 60 F254 230-400 mesh. Thin-layer chromatography (TLC) was performed on aluminum backed silica plates (0.2 mm, 60 F254). Visualization of the developed chromatogram was performed by fluorescence quenching, using phosphomolybdic acid, anisaldehyde or potassium permanganate stains. Mass spectra (ESI) were recorded on a Finningan® Surveyor MSQ LC-MS spectrometer. HRMS spectra were recorded on Bruker® Maxis Impact QTOF spectrometer. 1H and 13C NMR spectra were recorded on Varian® Mercury (200 MHz and 50 MHz respectively), or a Bruker® Avance (500 MHz and 125 MHz), and are internally referenced to residual solvent signals. Data for 1H NMR are reported as follows: chemical shift (δ ppm), integration, multiplicity (s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet, br s = broad singlet), coupling constant and assignment. -
2013 Pguy Acd Labs Presentation
‘Next Generation Fingerprinting’ A GC‐HR‐TOF‐MS Method to Semi‐Quantify Constituents in Aerosols and Aerosol Fractions E. Dossin, A. Monge, E. Martin, P. Pospisil, A. Knorr, M.C. Bentley, P.A. Guy Metabolomics & Analytical Chemistry Gr., Philip Morris Products SA, 2000 Neuchatel, Switzerland Outline 1. Description of the existing GC-MS fingerprinting method Pros & cons of the current fingerprinting method Why switching to a 7200 Agilent high resolution MS instrument? 2. How to tackle semi-quantification of the smoke constituents with the help of chemoinformatics tools Curation step for smoke constituents to be monitored Analysis of reference standards Retention time prediction model (QSPR approach) Selection of appropriate internal standards (clustering approach) 3. Semi-quantification from calibration curve of reference standards Linearity Assessment of silylation 4. What about other smoke constituents? 5. Conclusion Page: 2 Existing Fingerprinting Method • Aerosol sample generated from a smoking machine (ISO) – Whole smoke – Gas Vapor Phase (GVP) sbPBS – Total Particulate Matter (TPM) • Compounds list • GC columns (HP6890 GC) – DB-624: HS-SPME-GC-MS Volatile Chemicals – DB-FFAP: GC-MS Non Polar Chemicals –DB-5-MS: HT-GC-MS Polar Chemicals (TMS) • Detection (MSD5973 MS) – Electron ionization mode – Full scan (low resolution) Semi-quantification (d6-phenol) Page: 3 Description of the Former GC‐MS Fingerprinting Method (HP6890 GC ‐ MSD5973 MS) Cell culture Medium plus Cigarette DB-624 column ● Headspace(HS)-SPME-GC-MS Smoke high -
List of Extremely Hazardous Substances
Emergency Planning and Community Right-to-Know Facility Reporting Compliance Manual List of Extremely Hazardous Substances Threshold Threshold Quantity (TQ) Reportable Planning (pounds) Quantity Quantity (Industry Use (pounds) (pounds) CAS # Chemical Name Only) (Spill/Release) (LEPC Use Only) 75-86-5 Acetone Cyanohydrin 500 10 1,000 1752-30-3 Acetone Thiosemicarbazide 500/500 1,000 1,000/10,000 107-02-8 Acrolein 500 1 500 79-06-1 Acrylamide 500/500 5,000 1,000/10,000 107-13-1 Acrylonitrile 500 100 10,000 814-68-6 Acrylyl Chloride 100 100 100 111-69-3 Adiponitrile 500 1,000 1,000 116-06-3 Aldicarb 100/500 1 100/10,000 309-00-2 Aldrin 500/500 1 500/10,000 107-18-6 Allyl Alcohol 500 100 1,000 107-11-9 Allylamine 500 500 500 20859-73-8 Aluminum Phosphide 500 100 500 54-62-6 Aminopterin 500/500 500 500/10,000 78-53-5 Amiton 500 500 500 3734-97-2 Amiton Oxalate 100/500 100 100/10,000 7664-41-7 Ammonia 500 100 500 300-62-9 Amphetamine 500 1,000 1,000 62-53-3 Aniline 500 5,000 1,000 88-05-1 Aniline, 2,4,6-trimethyl- 500 500 500 7783-70-2 Antimony pentafluoride 500 500 500 1397-94-0 Antimycin A 500/500 1,000 1,000/10,000 86-88-4 ANTU 500/500 100 500/10,000 1303-28-2 Arsenic pentoxide 100/500 1 100/10,000 1327-53-3 Arsenous oxide 100/500 1 100/10,000 7784-34-1 Arsenous trichloride 500 1 500 7784-42-1 Arsine 100 100 100 2642-71-9 Azinphos-Ethyl 100/500 100 100/10,000 86-50-0 Azinphos-Methyl 10/500 1 10/10,000 98-87-3 Benzal Chloride 500 5,000 500 98-16-8 Benzenamine, 3-(trifluoromethyl)- 500 500 500 100-14-1 Benzene, 1-(chloromethyl)-4-nitro- 500/500 -
(12) United States Patent (10) Patent N0.: US 7,265,155 B2 Artman Et A1
US007265155B2 (12) United States Patent (10) Patent N0.: US 7,265,155 B2 Artman et a1. (45) Date of Patent: *Sep. 4, 2007 (54) TREATING A VARIETY OF PATHOLOGICAL W0 98 08498 A 3/1998 CONDITIONS, INCLUDING SPASTICITY WO WO98/08498 3/1998 AND CONVULSIONS, BY EFFECTING A WO WO99/44623 3/1999 MODULATION OF CNS ACTIVITY WITH W0 WO 01/28516 10/2000 ISOVALERAMIDE, ISOVALERIC ACID, OR A RELATED COMPOUND OTHER PUBLICATIONS Schon and Blau, J Neurol Neurosurg Psychiatry, Sep. 1987: (75) Inventors: Linda D. Artman, Salt Lake City, UT 50(9):1148-1152.* (US); Manuel Balandrin, Sandy, UT Dorland’s Medical Dictionary 27th ed. p. 379* (US); Robert L. Smith, Lansdale, PA Pharmacotherapy, A Pathophysiologic Approach, Dipiro et al.2nd (Us) ed. 1991, pp. 1232, 1238).* Drug facts and comparisons 1999 ed. pp. 1595-1597(“Drug (73) Assignee: NBS Pharmaceuticals, Inc., Salt Lake Facts”).* City, UT (US) Pharmacotherapy, A Pathophysiologic Approach, Dipiro et al. 2nd ed. 1991, pp. 1232 & 1238* Notice: Subject to any disclaimer, the term of this Drug Facts and Comparisons. 1999 ed. pp. 1595-1597 (“Drug patent is extended or adjusted under 35 Facts”).* Julius A. Vida “Advances in Anticonvulsant Drug Development”; USC 154(b) by 0 days. Anticonvulsants (1997) pp. 1-9; Academic Press. Julius A. Vida “Noncyclic Anticonvulsants”; Anticonvulsants This patent is subject to a terminal dis (1977) pp. 577-619; Academic Press. claimer. Salim Hadad, et al. “Pharmacokinetic Analysis and Antiepileptic Activity of N-Valproyl Deriatives of GABA and Glycine”; Phar (21) Appl. N0.: 10/614,344 maceutical Research (1995), pp. 905-907; Plenum Publishing Cor poration. -
List of Lists
United States Office of Solid Waste EPA 550-B-10-001 Environmental Protection and Emergency Response May 2010 Agency www.epa.gov/emergencies LIST OF LISTS Consolidated List of Chemicals Subject to the Emergency Planning and Community Right- To-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act • EPCRA Section 302 Extremely Hazardous Substances • CERCLA Hazardous Substances • EPCRA Section 313 Toxic Chemicals • CAA 112(r) Regulated Chemicals For Accidental Release Prevention Office of Emergency Management This page intentionally left blank. TABLE OF CONTENTS Page Introduction................................................................................................................................................ i List of Lists – Conslidated List of Chemicals (by CAS #) Subject to the Emergency Planning and Community Right-to-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act ................................................. 1 Appendix A: Alphabetical Listing of Consolidated List ..................................................................... A-1 Appendix B: Radionuclides Listed Under CERCLA .......................................................................... B-1 Appendix C: RCRA Waste Streams and Unlisted Hazardous Wastes................................................ C-1 This page intentionally left blank. LIST OF LISTS Consolidated List of Chemicals -
Laboratory and Chemical Storage Areas Must Be Kept Locked When Not in Use
CHEMICAL HYGIENE PLAN AND HAZARDOUS MATERIALS SAFETY MANUAL FOR LABORATORIES This is the Chemical Hygiene Plan specific to the following areas: Laboratory name or room number(s): ___________________________________ Building: __________________________________________________________ Supervisor: _______________________________________________________ Department: _______________________________________________________ EMERGENCY TELEPHONE NUMBERS: 911 for Emergency and urgent consultation 3-2035 MSU Police; 3-2066 Facilities Management 3-2179 or (606) 207-0629 Eddie Frazier, Director of Risk Management 3-2584 or (606) 207-9425 Holly Niehoff, Environmental Health & Safety Specialist 3-2099 Derek Lewis, Environmental Health & Safety Technician 3-______ Building Supervisor State 24-hour warning point for HAZMAT Spill Notification If you need to report a spill in accordance with SARA Title III Section 304 and KRS 39E.190, please contact the Duty Officer at the Commonwealth Emergency Operations Center at 800.255.2587 which serves as the twenty-four (24) hour warning point and contact for the Commonwealth Emergency Response Commission. Updated 2018 All laboratory chemical use areas must maintain a work-area specific Chemical Hygiene Plan which conforms to the requirements of the OSHA Laboratory Standard 29 CFR 19190.1450. Morehead State UniversityMorehead laboratories State may Chemical use this document Hygiene Plan as a starting point for creating their work area specific Chemical Hygiene Plan (CHP). MSU Laboratory Awareness Certification For CHP of (Professor, Building, Room)________________________ The Occupational Safety and Health Administration (OSHA) requires that laboratory employees be made aware of the Chemical Hygiene Plan at their place of employment (29 CFR 1910.1450). The Morehead State University Chemical Hygiene Plan and Hazardous Materials Safety Manual serves as the written Chemical Hygiene Plan (CHP) for laboratories using chemicals at Morehead State University. -
Basics of Pump-And-Treat Ground-Water Remediation Technology
United States Robert S. Kerr EPA/600/8-90/003 Environmental Protection Environmental Research Laboratory March 1990 Agency Ada OK 74820 Research and Development Basics of Pump-and-Treat Ground-Water Remediation Technology Word-searchable version – Not a true copy EPA-600/8-90/003 Basics of Pump-and-Treat Ground-Water Remediation Technology James W. Mercer, David C. Skipp and Daniel Giffin Geo Trans, Inc. 250-A Exchange Place Herndon, Virginia 22070 Project Officer Randall R. Ross Extramural Activities and Assistance Division Robert S. Kerr Environmental Research Laboratory Office of Research and Development U.S. Environment Protection Agency Ada, Oklahoma 74820 Word-Searchable Version – Not a true copy Disclaimer The Information in this document has been funded in part by the United States Environmental Protection Agency under Contract No. 68-C8-0058 to Dynamac Corporation. It has been subjected to the Agency's peer and administrative review, and it has been approved for publication as an EPA document. Mention of trade names or commercial products does not constitute endorsement or recommendation for use. ii Word-searchable version – Not a true copy Foreword EPA is charged by Congress to protect the nation's land, air and water systems. Under a mandate of national environmental laws focused on air and water quality, solid waste management and the control of toxic substances, pesticides, noise and radiation, the Agency strives to formulate and implement actions which lead to a compatible balance between human activities and the ability of natural systems to support and nurture life. The Robert S. Kerr Environmental Research Laboratory is the Agency's center of expertise for investigation of the soil and subsurface environment. -
Environmental Protection Agency Pt. 355, App. B
Environmental Protection Agency Pt. 355, App. B [Alphabetical Order] Reportable Threshold plan- CAS No. Chemical name Notes quantity * ning quantity (pounds) (pounds) 5344–82–1 ............ Thiourea, (2-Chlorophenyl)- ....................................... ..................... 100 100/10,000 614–78–8 .............. Thiourea, (2-Methylphenyl)- ....................................... ..................... 500 500/10,000 7550–45–0 ............ Titanium Tetrachloride ................................................ ..................... 1,000 100 584–84–9 .............. Toluene 2,4-Diisocyanate ........................................... ..................... 100 500 91–08–7 ................ Toluene 2,6-Diisocyanate ........................................... ..................... 100 100 110–57–6 .............. Trans-1,4-Dichlorobutene ........................................... ..................... 500 500 1031–47–6 ............ Triamiphos .................................................................. ..................... 500 500/10,000 24017–47–8 .......... Triazofos ..................................................................... ..................... 500 500 76–02–8 ................ Trichloroacetyl Chloride .............................................. ..................... 500 500 115–21–9 .............. Trichloroethylsilane ..................................................... d .................. 500 500 327–98–0 .............. Trichloronate ............................................................... e ................. -
395 B 536 Winstal. O. Saito EEEEEE
USOO8426439B2 (12) UnitedO States Patent (10) Patent No.: US 8.426,439 B2 Ciccocioppo (45) Date of Patent: *Apr. 23, 2013 (54) COMPOSITIONS AND METHODS FOR 7,510,728 B2 3/2009 Koike ........................... 424/464 PROPHYLAXIS AND TREATMENT OF 7,517,900 B2 4/2009 Pendri et al. ... 514,404 7,524,975 B2 4/2009 Mae et al. ... 549,405 ADDCTIONS 2002fOOO6942 A1 1/2002 Davis ........... ... 514,369 2002fOO77320 A1 6/2002 Lohray et al. 514/226.2 (75) Inventor: Roberto Ciccocioppo, Camerino (IT) 2003/0069246 A1 4/2003 Darrow et al. ................ 514,245 2003/010.0587 A1 5/2003 Moinet et al. ................. 514,369 (73) Assignee: Omeros Corporation, Seattle, WA (US) 2003/0220373 Al 1 1/2003 Jaye et al. ... 514,342 2004/0028735 A1 2/2004 Kositprapa ... 424/468 2004/OO77525 A1 4/2004 Chapman et al. ... 514/2 - r 2004/0096499 A1 5/2004 Vaya et al. ... 424/468 (*) Notice: Subject to any disclaimer, the term of this 2004/0127443 A1 7/2004 Pershadsingh 514,44 patent is extended or adjusted under 35 2004/0204472 A1 10/2004 Briggs et al. 514,406 U.S.C. 154(b) by 859 days. 2005, 00041 79 A1 1/2005 Pedersen ...... ... 514,342 2005, OO14786 A1 1/2005 Sun et al. .. ... 514/313 This patent is Subject to a terminal dis- 2005, OO 14833 A1 1/2005 Clark et al. .. ... 514,561 claimer. 2005, 0096331 A1 5/2005 Das et al. 514,259.3 2005, 01711.1.0 A1 8, 2005 Yu et al. ....... ... 514,248 2006, OOO9518 A1 1/2006 Campbell et al. -
Thermochemical Properties and Regularities of Amides, Anilides
DOI: 10.17344/acsi.2017.3683 Acta Chim. Slov. 2018, 65, 127–130 127 Scientific paper Thermochemical Properties and Regularities of Amides, Anilides, and Amidic Acids Alma Kairlapovna Ryskaliyeva,* Murat Ergalievich Baltabayev and Aigul Moldakhmetovna Zhubatova Kazakh National Agrarian University, 8 Abay Av., 050000 Almaty, Kazakhstan * Corresponding author: E-mail: [email protected] Received: 08-07-2017 Abstract The thermodynamic properties of carbamide and its alkyl substituted were studied insufficiently. In this article, the en- thalpies of combustion of ΔсН of some amides, anilides and amidic acids have been determined experimentally; their standard enthalpies of formation have been calculated. Linear dependences between the average atomic enthalpy of + combustion of ΔcH amides and their basicity constants in acidic aqueous solutions of pKBH have been established; a correlation that relates the enthalpies of combustion of amides and the corresponding amidic acids has been found. Keywords: Enthalpy of combustion, thermochemistry, amides, correlation analysis 3 1. Introduction self-packing calorimetric bomb (Vint. = 325 cm ), equipped with two valves (for input and output of gases), was used to Amides, anilides and their derivatives play an im- determine the enthalpies of combustion of the studied portant role in various biochemical processes and are compounds. The measurement error of the calorimeter therefore widely used as analytical and organic reagents in was ± 0.1%, which was absolutely insufficient to make pre- plant growing,